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Nakcheol Jeong - Publications

Affiliations: 
1987 Princeton University, Princeton, NJ 
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39 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Han J, Kim S, Lee MS, Kim M, Jeong N. Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks (MOFs). Journal of Visualized Experiments : Jove. PMID 32009645 DOI: 10.3791/60624  0.413
2019 Han J, Lee MS, Thallapally PK, Kim M, Jeong N. Identification of Reaction Sites on Metal–Organic Framework-Based Asymmetric Catalysts for Carbonyl–Ene Reactions Acs Catalysis. 9: 3969-3977. DOI: 10.1021/Acscatal.8B04827  0.391
2018 Lee JH, El-Damasy AK, Seo SH, Gadhe CG, Pae AN, Jeong N, Hong SS, Keum G. Novel 5,6-disubstituted pyrrolo[2,3-d]pyrimidine derivatives as broad spectrum antiproliferative agents: Synthesis, cell based assays, kinase profile and molecular docking study. Bioorganic & Medicinal Chemistry. PMID 30385226 DOI: 10.1016/J.Bmc.2018.10.004  0.396
2015 Lee M, Shin SM, Jeong N, Thallapally PK. Chiral environment of catalytic sites in the chiral metal-organic frameworks. Dalton Transactions (Cambridge, England : 2003). 44: 9349-52. PMID 25912165 DOI: 10.1039/C5Dt01322D  0.341
2015 Furusawa T, Morimoto T, Ikeda K, Tanimoto H, Nishiyama Y, Kakiuchi K, Jeong N. Asymmetric Pauson-Khand-type reactions of 1,6-enynes using formaldehyde as a carbonyl source by cooperative dual rhodium catalysis Tetrahedron. 71: 875-881. DOI: 10.1016/J.Tet.2014.12.038  0.419
2015 Lee MS, Shin SM, Kim HJ, Jeong N. Enantioselective carbonyl-ene reaction catalyzed by chiral metal-organic framework-based heterogeneous catalyst Bulletin of the Korean Chemical Society. 36: 1282-1284. DOI: 10.1002/Bkcs.10228  0.398
2014 Bhattarai D, Lee JH, Seo SH, Nam G, Choo H, Kang SB, Kwak JH, Oh T, Cho SN, Pae AN, Kim EE, Jeong N, Keum G. Synthesis and in vitro evaluation of the antitubercular and antibacterial activity of novel oxazolidinones bearing octahydrocyclopenta[c]pyrrol-2-yl moieties. Chemical & Pharmaceutical Bulletin. 62: 1214-24. PMID 25297523 DOI: 10.1248/Cpb.C14-00510  0.393
2014 Lee JH, Seo SH, Lim EJ, Cho NC, Nam G, Kang SB, Pae AN, Jeong N, Keum G. Synthesis and biological evaluation of 1-(isoxazol-5-ylmethylaminoethyl)-4-phenyl tetrahydropyridine and piperidine derivatives as potent T-type calcium channel blockers with antinociceptive effect in a neuropathic pain model. European Journal of Medicinal Chemistry. 74: 246-57. PMID 24480356 DOI: 10.1016/J.Ejmech.2013.12.056  0.377
2013 Li Q, Shin SM, Moon D, Jeong KS, Jeong N. Chiral porous metal-organic frameworks from chiral building units with different metrics Crystengcomm. 15: 10161-10164. DOI: 10.1039/C3Ce41586D  0.326
2011 Kim DE, Park SH, Choi YH, Lee SG, Moon D, Seo J, Jeong N. Internal chelation-guided regio- and stereoselective Pauson-Khand-type reaction by chiral rhodium(I) catalysis. Chemistry, An Asian Journal. 6: 2009-14. PMID 21678560 DOI: 10.1002/Asia.201100271  0.418
2011 Jeong KS, Go YB, Shin SM, Lee SJ, Kim J, Yaghi OM, Jeong N. Asymmetric catalytic reactions by NbO-type chiral metal-organic frameworks Chemical Science. 2: 877-882. DOI: 10.1039/C0Sc00582G  0.448
2011 Jeong KS, Lee BH, Li Q, Choi SB, Kim J, Jeong N. Near achiral metal-organic frameworks from conformationally flexible homochiral ligands resulted by the preferential formation of pseudo-inversion center in asymmetric unit Crystengcomm. 13: 1277-1279. DOI: 10.1039/C0Ce00426J  0.336
2010 Han M, Nam KD, Shin D, Jeong N, Hahn HG. Exploration of novel 2-alkylimino-1,3-thiazolines: T-type calcium channel inhibitory activity. Journal of Combinatorial Chemistry. 12: 518-30. PMID 20450201 DOI: 10.1021/Cc100041M  0.315
2010 Kim DE, Ratovelomanana-Vidal V, Jeong N. 2,2′-bis[bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphino]-6, 6′-dimethoxy- 1,1′-biphenyl in intramolecular rhodium(I)-catalyzed asymmetric Pauson-Khand-type reactions Advanced Synthesis and Catalysis. 352: 2032-2040. DOI: 10.1002/Adsc.201000221  0.456
2009 Choi YH, Kwak J, Jeong N. Solvent effects on the asymmetric Pauson–Khand-type reaction by rhodium Tetrahedron Letters. 50: 6068-6071. DOI: 10.1016/J.Tetlet.2009.08.060  0.407
2009 Kim DE, Kwak J, Kim IS, Jeong N. Kinetic Resolutions by Enantioselective Pauson–Khand‐Type Reaction Advanced Synthesis & Catalysis. 351: 97-102. DOI: 10.1002/Adsc.200800657  0.409
2008 Kim DE, Kim IS, Ratovelomanana-Vidal V, Genêt JP, Jeong N. Asymmetric Pauson-Khand-type reaction mediated by Rh(I) catalyst at ambient temperature. The Journal of Organic Chemistry. 73: 7985-9. PMID 18798672 DOI: 10.1021/Jo801236C  0.378
2008 Kim DE, Lee BH, Rajagopalasarma M, Genêt J, Ratovelomanana-Vidal V, Jeong N. Asymmetric Desymmetrization of the Diallyl Acetals of Alkynals by the Enantioselective Pauson-Khand-Type Reaction Catalysts Advanced Synthesis & Catalysis. 350: 2695-2700. DOI: 10.1002/Adsc.200800514  0.424
2007 Kim DE, Choi C, Kim IS, Jeulin S, Ratovelomanana-Vidal V, Genêt JP, Jeong N. Electronic and Steric Effects of Atropisomeric Ligands SYNPHOS® and DIFLUORPHOS®vs. BINAPs in Rh(I)-Catalyzed Asymmetric Pauson–Khand Reaction Advanced Synthesis & Catalysis. 349: 1999-2006. DOI: 10.1002/Adsc.200600623  0.358
2006 Kim DE, Choi C, Kim IS, Jeulin S, Ratovelomanana-Vidal V, Genêt JP, Jeong N. The Electronic Effect of Ligands on Stereoselectivity in the Rhodium(I)-Catalyzed Asymmetric Pauson–Khand-Type Reaction under a Carbon Monoxide Atmosphere Synthesis. 2006: 4053-4059. DOI: 10.1055/S-2006-950369  0.398
2005 Jeong KS, Kim SY, Shin US, Kogej M, Hai NT, Broekmann P, Jeong N, Kirchner B, Reiher M, Schalley CA. Synthesis of chiral self-assembling rhombs and their characterization in solution, in the gas phase, and at the liquid-solid interface. Journal of the American Chemical Society. 127: 17672-85. PMID 16351097 DOI: 10.1021/Ja053781I  0.307
2004 Jeong N, Kim DH, Choi JH. Desymmetrization of meso-dienyne by asymmetric Pauson-Khand type reaction catalysts. Chemical Communications (Cambridge, England). 1134-5. PMID 15116221 DOI: 10.1039/B401288G  0.416
2004 Stumpf A, Hwang SH, Kim JS, Jeong N. Asymmetric addition of bis(homoally)zinc to the propargyl aldehyde dicobalt hexacarbonyl complexes in the presence of chiral disulfonamide followed by Pauson-Khand reaction Bulletin of the Korean Chemical Society. 25: 1621-1622. DOI: 10.5012/Bkcs.2004.25.11.1621  0.383
2002 Jeong N, Sung BK, Kim JS, Park SB, Seo SD, Shin JY, In KY, Choi YK. Pauson­Khand-type reaction mediated by Rh(I) catalysts Pure and Applied Chemistry. 74: 85-91. DOI: 10.1351/Pac200274010085  0.424
2000 Jeong N, Hwang SH. Catalytic Intermolecular Pauson – Khand Reactions in Supercritical Ethylene Angewandte Chemie. 39: 636-638. PMID 10671283 DOI: 10.1002/(Sici)1521-3773(20000204)39:3<636::Aid-Anie636>3.0.Co;2-S  0.329
2000 Jeong N, Seo aSD, Shin JY. One Pot Preparation of Bicyclopentenones from Propargyl Malonates (and Propargylsulfonamides) and Allylic Acetates by a Tandem Action of Catalysts Journal of the American Chemical Society. 122: 10220-10221. DOI: 10.1021/Ja001750B  0.332
2000 Jeong N, Sung BK, Choi YK. Rhodium(I)-Catalyzed Asymmetric Intramolecular Pauson−Khand-Type Reaction Journal of the American Chemical Society. 122: 6771-6772. DOI: 10.1021/Ja0007049  0.411
1998 Jeong N, Lee S, Sung BK. Rhodium(I)-Catalyzed Intramolecular Pauson-Khand Reaction Organometallics. 17: 3642-3644. DOI: 10.1021/Om980410K  0.405
1997 Stumpf A, Jeong N, Sunghee H. 3-Thiabicyclo-3,3,0-Oct-5-En-7-Ones By Dmso/Dms Promoted Intramolecular Pauson-Khand Reaction Synlett. 1997: 205-207. DOI: 10.1055/S-1997-741  0.402
1997 Jeong N, Hwang SH, Lee YW, Lim JS. Catalytic Pauson−Khand Reaction in Super Critical Fluids Journal of the American Chemical Society. 119: 10549-10550. DOI: 10.1021/Ja972099O  0.348
1994 Jeong N, Hwang SH, Lee Y, Chung YK. Catalytic version of the Intramolecular Pauson-Khand Reaction Journal of the American Chemical Society. 116: 3159-3160. DOI: 10.1021/Ja00086A070  0.406
1994 Lee BY, Moon H, Chung YK, Jeong N. Generation of cyclopentadienyl ligands via the Pauson-Khand and Retro-Diels-Alder reactions Journal of the American Chemical Society. 116: 2163-2164. DOI: 10.1021/Ja00084A074  0.372
1993 Chung YK, Lee BY, Jeong N, Hudecek M, Pauson PL. Promoters for the (alkyne)hexacarbonyldicobalt-based cyclopentenone synthesis Organometallics. 12: 220-223. DOI: 10.1021/Om00025A036  0.374
1993 Jeong N, Lee SJ, Lee BY, Chung YK. Molybdenium mediated preparation of cyclopentenones Tetrahedron Letters. 34: 4027-4030. DOI: 10.1016/S0040-4039(00)60607-X  0.362
1993 Jeong N, Bun YL, Seong ML, Young KC, Sueg-Geun L. Preparations of bicycliclactols from allyl and/or homoallyl propargyl acetal-cobalt complexes and its application to the formal synthesis of (±) loganine Tetrahedron Letters. 34: 4023-4026. DOI: 10.1016/S0040-4039(00)60606-8  0.316
1991 Jeong N, Chung YK, Lee BY, Lee SH, Yoo SE. A Dramatic Acceleration of the Pauson-Khand Reaction by Trimethylamine N-Oxide1,2 Synlett. 1991: 204-206. DOI: 10.1055/S-1991-20681  0.33
1991 Jeong N, Yoo Se, Lee SJ, Lee SH, Chung YK. An efficient preparation of 3-azabicyclo [3.3.0]. Oct-5-en-7-ones from propargyl alcohol- cobalt complexes via nicholas reaction with amidic nitrogen nucleophiles followed by pauson-khand cyclization Tetrahedron Letters. 32: 2137-2140. DOI: 10.1016/S0040-4039(00)71257-3  0.361
1990 Berk SC, Yeh MCP, Jeong N, Knochel P. Preparation and Reactions of Functionalized Benzylic Organometallics of Zinc And Copper Organometallics. 9: 3053-3064. DOI: 10.1021/Om00162A016  0.468
1989 Knochel P, Jeong N, Rozema MJ, Yeh MCP. Zinc and copper carbenoids as efficient and selective a1/d1 multicoupling reagents. 1 Journal of the American Chemical Society. 111: 6474-6476. DOI: 10.1021/Ja00198A097  0.353
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